Hypertrophic Scarring After Facial Burn

NCT ID: NCT00242970

Last Updated: 2015-04-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

15 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-10-31

Study Completion Date

2011-02-28

Brief Summary

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Subjects with a burn to the face and/or neck will be enrolled into the study and a Three-Dimensional scanner used to see if it can objectively measure scar color and volume and measure the effect of scar on motion of the face and neck.

Detailed Description

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Subjects will have 11 clinic visits over a 2-year period. An initial scan of the subject's head and neck will be made. Ten reproducible landmarks on the face and neck will be determined. The subject will return for follow up scans at Day 14, Day 28 and Month 2,6,9,12,18 and 24.

Conditions

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Burn

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Interventions

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3-Dimensional Color Scanning

Color imaging of the face and neck.

Intervention Type DEVICE

Other Intervention Names

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Cyberware 3030 RGB Color Scanner

Eligibility Criteria

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Inclusion Criteria

* Face and/or Neck Burn
Minimum Eligible Age

4 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Total Contact

UNKNOWN

Sponsor Role collaborator

Legacy Health System

OTHER

Sponsor Role lead

Responsible Party

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Helens Christians

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Helen Christians, ORT/L

Role: PRINCIPAL_INVESTIGATOR

Legacy Health System

Locations

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Legacy Emanuel Hospital and Health Center

Portland, Oregon, United States

Site Status

Countries

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United States

Other Identifiers

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OBC3DS-01

Identifier Type: -

Identifier Source: org_study_id

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